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Ethanol → HCID 178489016, 화합물

HRID 584747
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HRID 584747 반응식
[CH3:1][O:2][C:3]1[CH:23]=[CH:22][C:6]([C:7]([N:9]([C:14]2[CH:15]=[N:16][C:17]([O:20][CH3:21])=[CH:18][CH:19]=2)[NH:10][C:11]([NH2:13])=[O:12])=O)=[CH:5][CH:4]=1.C(O)C>[OH-].[Na+]>[CH3:1][O:2][C:3]1[CH:23]=[CH:22][C:6]([C:7]2[N:9]([C:14]3[CH:15]=[N:16][C:17]([O:20][CH3:21])=[CH:18][CH:19]=3)[N:10]=[C:11]([OH:12])[N:13]=2)=[CH:5][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 702EthanolHCID 22341584HCID 22341584, 화합물

생성물 1

HCID 178489016HCID 178489016, 화합물수율 72.7%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

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온도
60 °C

실험 절차

A mixture of 2-(4-methoxybenzoyl)-2-(6-methoxypyridin-3-yl)hydrazinecarboxamide (1.0 g, 3.16 mmol) in 10% sodium hydroxide solution (2 mL)-ethanol (3mL) was heated at 60° C. for 1.5 hours. After cooling, the solvent was removed under reduced pressure. Water was added to the residue and the mixture was adjusted pH to ca. 4 to 5. A generated precipitate was isolated by filtration, washed with water and small amount of ethyl acetate, dried in vacuo to give 5-(4-methoxyphenyl)-1-(6-methoxypyridin-3-yl)-1H-1,2,4-triazol-3-ol (685 mg, 72.6% yield).

후처리

  1. temperatureAfter cooling
  2. customthe solvent was removed under reduced pressure
  3. additionWater was added to the residue
  4. customA generated precipitate was isolated by filtration
  5. washwashed with water and small amount of ethyl acetate
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-7bd22ab8fced4ae1a222dc44ec2adb20
출처 데이터셋
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06927230B2

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